CSF Tau, Abeta42, and MHPG Differentiate Dementia with Lewy Bodies from Alzheimer's Disease
SourceJournal of Alzheimer's Disease, 27, 2, (2011), pp. 377-84
Article / Letter to editor
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Laboratory of Genetic, Endocrine and Metabolic Diseases
Journal of Alzheimer's Disease
SubjectDCN 1: Perception and Action NCEBP 11: Alzheimer Centre; DCN 2: Functional Neurogenomics; DCN 2: Functional Neurogenomics NCEBP 10: Human Movement & Fatigue; N4i 1: Pathogenesis and modulation of inflammation; NCEBP 14: Cardiovascular diseases
Differentiating dementia with Lewy bodies (DLB) from Alzheimer's Disease (AD) can be difficult because of the substantial overlap in clinical features. Since deficits in serotonergic and dopaminergic pathways seem more pronounced in DLB patients, we investigated whether cerebrospinal fluid (CSF) analysis of neurotransmitter metabolites, in addition to brain-specific proteins, may improve the differentiation between DLB and AD. We retrospectively compared CSF concentrations of the neurotransmitter metabolites homovanillic acid (HVA), 5-hydroxyindolacetic acid (5-HIAA), and 3-methoxy-4-hydroxyphenylethyleneglycol (MHPG) and the brain-specific proteins total tau (t-tau), phosphorylated tau protein (p-tau), and amyloid-beta42 (Abeta42) in 45 patients with AD (mean age 71.6 years; 34 (76%) men; 44 probable AD, 1 definite) and 23 patients with DLB (mean age 71.6 years; 18 (78%) men; 6 possible DLB, 16 probable, 1 definite). The concentrations of all neurotransmitter metabolites, as well as those for t-tau and p-tau protein, were significantly lower in DLB compared to AD, irrespective of the diagnostic certainty (i.e., possible or probable). The currently used combination of Abeta42, p-tau, and t-tau yielded a sensitivity of 92.9% and a specificity of 90%. The addition of MHPG resulted in an increased sensitivity of 97.6% and a specificity of 95% for the discrimination between DLB and AD. In conclusion, the combination of MHPG and the brain specific proteins t-tau, p-tau, and Abeta42 in CSF were associated with the clinical diagnosis of DLB and discriminated between AD and DLB with high diagnostic accuracy, suggesting this combination as a potential biomarker for DLB.
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